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Rural Libraries Promoting Walking and Walkability in Their Rural Communities

Rural Libraries Promoting Walking and Walkability in Their Rural Communities

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05677906
Enrollment
331
Registered
2023-01-10
Start date
2023-04-25
Completion date
2025-12-31
Last updated
2024-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Activity

Keywords

rural populations, physical activity promotion

Brief summary

The investigators will randomize 20 rural libraries to implement either a group-based walking (standard approach) or a group-based walking combined with a civic engagement program (combined approach). Each rural library will enroll between 15-20 participants. The investigators will compare the change in physical activity between participants in each group.

Detailed description

The goals of this study are: 1. Increase the capacity of rural libraries to deliver evidence-based health promotion programs 2. Compare the effects of a group-based walking program with a combined group-based plus civic engagement program on physical activity, cardiovascular fitness and collective efficacy among rural residents. 3. Evaluate program implementation

Interventions

OTHERWalking only (Step It Up!)

Participants will meet weekly for 60 minutes and walk together as a group. Participants will progressively build up to walking for 45 minutes at a brisk pace. Walks will start with a check-in and end with stretching as a group.

OTHERCombined (Step It Up! plus Civic Engagement)

Participants in the combined groups will meet weekly for 90 minutes with group members. They will participate in a group walk for 60 minutes followed by 30 minutes of civic engagement aimed at improving walkability in the community

Sponsors

Texas A&M University
CollaboratorOTHER
University of North Carolina, Greensboro
CollaboratorOTHER
Oregon Health and Science University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 18 or older * Inactive (defined as engaging in physical activity \<3 days per week) * Ability to walk for at least 20 minutes * Living within the rural community served by the local library * Ability to travel to the local library/location of walking group.

Exclusion criteria

* Participation/intention to participate in other lifestyle modification pro-gram(s) * Cognitive impairment * Inability to communicate due to severe uncorrected hearing loss or speech disorder or severe visual impairment (if precludes completion of assessments and/or intervention)

Design outcomes

Primary

MeasureTime frameDescription
Physical activityChange from baseline physical activity at 6 months, 12 months, and 24 months.Participants will be asked to wear an accelerometer for \>10 hours/day for seven days at the wrist to measure physical activity. An accelerometer is a small device worn at the wrist that records acceleration, the change in velocity of a participant over time.
Cardio respiratory fitnessChange from baseline cardio respiratory fitness at 6 months, 12 months, and 24 months.Participants will be asked to complete a six-minute walk test to measure cardiorespiratory fitness. The distance walked in 6 minutes will be recorded.
Collective EfficacyChange from baseline collective efficacy at 6 months, 12 months, and 24 monthsParticipants will be asked to complete a survey regarding collective-efficacy, the Collective Efficacy Scale (Sampson and colleagues, 1997), which measures how well communities work together to make things happen.

Secondary

MeasureTime frameDescription
WeightChange from baseline weight at 6 months, 12 months, and 24 months.Researchers will measure the weight of participants in pounds.
HeightBaselineResearchers will measure the height of participants in inches.
Blood pressureChange from baseline blood pressure at 6 months, 12 months, and 24 months.Researchers will measure the both diastolic and systolic blood pressure of participants using a sphygmomanometer.
Hip circumferenceChange from baseline hip circumference at 6 months, 12 months, and 24 months.Researchers will measure the hip circumference of participants in inches.
Resting heart rateChange from baseline resting heart rate at 6 months, 12 months, and 24 months.Researchers will measure resting heart rate of participants by using heart rate monitor.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026